48,XXXY Syndrome

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Medical EditorDr. Nicholas Bush MBBS BSc (Hons)

2 min read

Last Updated: 8 August 2024

48,XXXY Syndrome

48,XXXY syndrome is a rare genetic disorder affecting males, marked by the presence of two additional X chromosomes. Common symptoms include intellectual disability, distinctive facial features, and underdeveloped secondary sexual characteristics. Early diagnosis and supportive therapies can significantly improve quality of life for those with 48,XXXY syndrome.

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Trusted Resources

National Institute of Health (NIH)

48,XXXY Syndrome

In conclusion

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